chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
6
127596626
127596627
T
A
15
GENIC
homozygous
143993981
6
127598130
127598131
C
T
21
GENIC
homozygous
143993982
6
127598206
127598207
A
T
15
GENIC
homozygous
143993983
6
127599957
127599958
C
T
35
GENIC
homozygous
143993984
6
127600208
127600209
T
C
28
GENIC
homozygous
143993985
6
127600534
127600535
G
T
20
GENIC
homozygous
143993986
6
127601517
127601518
C
A
8
GENIC
homozygous
404000759
6
127601517
127601518
C
8
GENIC
heterozygous
404000760
6
127601682
127601683
T
C
16
GENIC
homozygous
143993987
6
127605407
127605408
G
A
10
GENIC
homozygous
143993988
6
127605431
127605432
C
T
10
GENIC
homozygous
143993989
6
127610393
127610394
T
10
GENIC
heterozygous
143977441
6
127601519
127601520
T
A
8
GENIC
homozygous
404000761
6
127601519
127601520
T
8
GENIC
heterozygous
404000762
6
127602885
127602885
G
28
GENIC
homozygous
143977438
6
127604635
127604639
AAAC
23
GENIC
heterozygous
143977439
6
127605234
127605234
AGTGCTCCCTCAGACAGTAGACCAG
16
GENIC
homozygous
143977440
6
127611869
127611870
G
A
19
GENIC
homozygous
143993990
6
127611939
127611940
A
G
19
GENIC
homozygous
143993991
6
127612359
127612359
AGAAAGAGAGAAAGAAAGAAAGAA
7
GENIC
homozygous
143977442
6
127613271
127613272
T
G
10
GENIC
homozygous
143993992